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Severe AsthmaNCT06283290

PROPE Severe Asthma Study in Egypt

An observational study of Severe Asthma, run by AstraZeneca at 4 sites in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Asthma is a syndrome characterized by airway inflammation, reversible airway obstruction, and airway hyper-responsiveness. Patients present clinically with recurrent wheezing, shortness of breath, cough, and chest tightness. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Severe Asthma
How many people
201 participants
Where
4 sitesEgypt
Study dates
12 Mar 2024to 28 Nov 2024
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: The study population will include patients 18 years and older with severe asthma, per the definition of the GINA 2022 Guidelines [4]. Patients will be identified and invited to participate in the study consecutively as they attend their routine clinical visits at the included centers. To be included in the study, each patient should meet all the inclusion criteria and none of the exclusion criteria described in the sections below. In addition, patients should provide written, informed consent prior to any study-specific procedures or data collection. The enrolment period will be approximately 8 months or until the required number of patients has been included, whichever occurs first.

Who may be able to join

  • Male or female patient, aged 18 years or older by the time of study entry
  • Patient visiting a participating center for a routine clinical appointment
  • The patient is willing and able to provide a blood sample for IgE and eosinophil levels determination as part of their routine clinical visit
  • Patients with a diagnosis of severe asthma for at least one year as defined by:
  • Treatment with guidelines-suggested medications for Global Initiative for Asthma (3) steps 4-5 asthma
  • Patients (or their legal guardian) who voluntarily sign and date the informed consent form (ICF) prior to study entry

Who cannot join

  • Patients with a diagnosis of chronic obstructive pulmonary disease (COPD) or other chronic respiratory conditions beyond severe asthma
  • An acute or chronic condition that, by the investigator's decision, would limit the patient's ability to participate in this study
  • Patients who are currently under biologic therapy to treat their severe asthma

Trial locations and contacts

4 sites in 1 country.

Egypt4 sites
  • Research Site

    Alexandria

  • Research Site

    Cairo

  • Research Site

    Dakahlia, Dakahlia Governorate

  • Research Site

    Sharkia, Sharqia Province

Other trials in Egypt

About this study

Official title: Prevalence of the OCS Use Among Severe Asthma Patients in Egypt: A Nation-wide, Cross-Sectional, Multicenter Study

Asthma is a syndrome characterized by airway inflammation, reversible airway obstruction, and airway hyper-responsiveness. Patients present clinically with recurrent wheezing, shortness of breath, cough, and chest tightness. Asthma is a leading cause of morbidity with a global prevalence of approximately 300 million; it is estimated that the number of people with asthma may increase to 400 to 450 million people worldwide by 2025.

Severe asthma is not considered a single disease; instead, it is divided into several phenotypes, owing to the variety of inflammatory, clinical, and functional characteristics that it can present with. One of the proposed and most studied phenotypes is severe eosinophilic asthma. Patients with severe asthma that is accompanied by a high concentration of eosinophils require greater healthcare resource use, greater disease management costs, and a much more impaired QoL than those who do not present with raised eosinophilia.

Read more

While the number of targeted treatments for asthma management has been growing in recent years, the heterogeneity of clinical presentations, treatment responses, and inflammatory processes involved represent an added challenge for health care professionals. Thus, severe asthma management is a complex endeavor, and a thorough and up-to-date understanding of the pathophysiologic characteristics of the patient population promotes effective therapeutic decision-making.

This cross-sectional, multicenter study aims to determine the prevalence of oral corticosteroid (OCS) use among severe asthma patients who attend to different sites specialized in the management of severe asthma across Egypt. In addition, the prevalence of eosinophilic phenotype of blood eosinophil count ≥ 150 cells/mm3, prevalence of atopic phenotype, and asthma control will also be studied.

Read the detailed description

Asthma is a syndrome characterized by airway inflammation, reversible airway obstruction, and airway hyper-responsiveness. As a result, patients present clinically with recurrent wheezing, shortness of breath, cough, and chest tightness. Asthma is a leading cause of morbidity, with a global prevalence of approximately 300 million; it is estimated that the number of people with asthma may increase to 400 to 450 million people worldwide by 2025.

Despite the availability of multiple therapeutic options, 5-10% of asthmatic patients present with severe disease that is associated with substantial morbidity. Severe asthma patient, as defined by the Global Initiative for Asthma (GINA) 2022 guidelines, is the asthmatic patient that is uncontrolled despite adherence with maximal optimized therapy and treatment of contributing factors, or worsens with high dose treatment is stepped down. They stated that severe asthmatic patient requires therapeutic options for steps 4-5 to prevent them from becoming "uncontrolled" or remaining "uncontrolled" despite therapy Severe asthma is recognized as a major unmet need that poses a great burden on the healthcare system. While accounting for only a small proportion of the total asthmatic population, severe asthma-related costs are 1.7 to 4-fold higher than those observed in the mild-persistent asthma population and may represent up to 50% of the total asthma-associated healthcare costs. Severe asthma also has a high personal and social impact as patients with severe asthma typically present with greater levels of anxiety and depression, with measures of quality of life (QoL) being far worse in severe asthma than in mild or moderate asthma.

Most of asthma patients experiencing frequent exacerbations and significant limitations on their lung function and quality of life. Oral corticosteroid (OCS) has been a mainstay of severe asthma management for almost 60 years, helping patients manage their exacerbations. Clinical guidelines, including the Australian Asthma Handbook and the GINA guidelines, recommend adding low-dose maintenance OCS when all other conventional treatments have failed to control asthma, when adequate inhaler technique and adherence have been attained, and when other contributing factors have been ruled out. Additionally, short bursts of OCS (i.e. 5-10 days) are recommended to manage severe asthma exacerbations. OCS is currently used by more than 13.5 million people with severe asthma worldwide to manage exacerbations and avoid hospitalization. For patients, this cumulative, prolonged use of OCS is linked to disabling adverse effects that might further impair their quality of life. Serious health hazards, such as diabetes, osteoporosis, and heart disease, can result from long-term OCS usage. Limited published studies suggest OCS usage varies across countries. Also, recent registry data show that at least 25-60% of patients with severe asthma in affluent nations may at some point be prescribed OCS.

Severe asthma is not considered a single disease; instead, it is divided into several phenotypes, owing to the variety of inflammatory, clinical, and functional characteristics that can manifest on the patients. One of these proposed and most studied phenotypes is severe eosinophilic asthma. Eosinophils have long been recognized as a key element in asthmatic inflammation. This persistent airway inflammation is partly responsible for the high frequency of exacerbations seen in severe asthma. Patients with severe asthma accompanied by a high concentration of eosinophils require greater healthcare resource utilization, greater disease management costs, and a much more impaired QoL than those who do not present with raised eosinophilia.

Despite its impact, severe eosinophilic asthma is yet to be clearly defined. Peripheral blood eosinophil counts as high as 400 cells/mm3 have been linked to increased asthma exacerbations. Nevertheless, adult-onset asthma patients with blood eosinophil counts above a lower threshold (≥300 cells/mm3) already present with a distinct phenotype of severe asthma with frequent exacerbations and poor prognosis. Additionally, studies of anti-eosinophilic therapies indicate patients with blood eosinophil levels ≥300 cells/mm3 already benefit from the targeted treatment.

Although eosinophilic inflammation of the airways has been classically associated with allergic asthma (i.e., asthma that is triggered by an allergen), there is evidence that eosinophilia is present in the airways of severe asthmatic patients without the allergic disease. Contrary to early-onset eosinophilic asthma, adult-onset eosinophilic asthma frequently develops in the absence of allergen-dependent activation of Th2 lymphocytes, which suggests a mechanism of eosinophilic inflammation other than allergy. Late-onset asthmatics have also been found to present a lower rate of skin prick sensitization, indicating that eosinophilic airway inflammation and atopy are not fully concordant. Of note, asthma patients may present with atopy (i.e., elevated immunoglobulin E [IgE] levels), but no sensitization to common inhaled allergens and asthma without allergic etiology.

The number of targeted treatments for asthma management has been growing in recent years. Still, the heterogeneity of clinical presentations, treatment responses, and inflammatory processes involved represent an added challenge for health care professionals.

Conditions
Severe Asthma
Medical subject headings
Asthma

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. To describe the prevalence (frequency) of OCS use among severe asthma patients as defined by chronic treatment and/or bursts of OCS use.

    To describe the prevalence (frequency) of OCS use among severe asthma patients as defined by chronic treatment and/or bursts of OCS use.

    Measured: 12 Months

Secondary outcomes (9)
  1. To describe the demographic characteristics of severe eosinophilic asthma patients.

    To describe the demographic characteristics of severe eosinophilic asthma patients.

    Measured: 12 months

  2. To describe the clinical characteristics of severe eosinophilic asthma patients.

    Number of severe asthma exacerbations, as per the Official ATS/ERS Statement on Asthma Control, in the year (12 months) prior to study entry.

    Measured: 12 months

  3. To discover the average OCS dose per year used among severe asthma patients.

    To discover the average OCS dose per year used among severe asthma patients.

    Measured: 12 months

  4. To determine the prevalence of the eosinophilic phenotype

    To determine the prevalence of the eosinophilic phenotype as defined by a blood eosinophil count ≥300 cells/mm3 among severe asthma patients across Egypt.

    Measured: 60 months

  5. To determine the prevalence of the eosinophilic phenotype

    To determine the prevalence of the eosinophilic phenotype as defined by a blood eosinophil count ≥ 150 cells/mm3 among severe asthma patients across Egypt.

    Measured: 60 months

  6. To determine the prevalence of the total serum IgE

    To determine the prevalence of the total serum IgE > 100 IU/mL among severe asthma patients in Egypt.

    Measured: 12 months

  7. To determine the annual severe asthma exacerbation rate in the past twelve months among severe asthma patients in Egypt

    To determine the annual severe asthma exacerbation rate in the past twelve months among severe asthma patients in Egypt, as defined by ATS/ERS as events that require urgent action on the part of the patient and physician to prevent a serious outcome, such as hospitalization or death from asthma

    Measured: 12 months

  8. To evaluate asthma control of severe asthma patients

    To evaluate asthma control of severe asthma patients, as assessed by the GINA (Global Initiative for Asthma) assessment of asthma control questions.

    0 = Well Controlled

    1 - 2 = Partly controlled 3 - 4 = Uncontrolled.

    Measured: 12 months

  9. To evaluate comorbidities related to OCS use

    To evaluate comorbidities related to OCS use

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Feb 2024
  2. Study start12 Mar 2024
  3. Primary completion28 Nov 2024
  4. Study completion28 Nov 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
201 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06283290
Sponsor's protocol ID
D3250R00122
Status last verified
Sep 2025
First submitted
31 Jan 2024
Last updated
26 Sep 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Severe Asthma, run by AstraZeneca at 4 sites in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 4 sites in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

To describe the prevalence (frequency) of OCS use among severe asthma patients as defined by chronic treatment and/or bursts of OCS use. (time frame: 12 Months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Sep 2025.

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